Building Blocks

<p>3-Bromofuran is a synthetic chemical that can be used to treat cancer, specifically as an anti-cancer agent. 3-Bromofuran has been shown to inhibit the growth of tumour cells in culture. It also selectively inhibits antigen expression and induces apoptosis in tumour cells. 3-Bromofuran is synthesized by a Sharpless asymmetric dihydroxylation of hippuric acid and efficiently undergoes cross coupling reactions with electron deficient polyatomic molecules such as organoaluminium compounds. The major metabolite of 3-bromofuran is 3,4-dihydroxybenzoic acid (3,4-DHBA), which has been found to have antiviral and antibacterial properties.</p>

<p>cis-N-(3-Chloroallyl)-1-(R)-aminoindan hydrochloride is a high quality, research chemical that is a versatile building block. It is used as a reagent and reaction component for the synthesis of fine chemicals, speciality chemicals, and complex compounds. cis-N-(3-Chloroallyl)-1-(R)-aminoindan hydrochloride has CAS number 1175018-80-0.</p>

<p>Ethyl 2-amino-4-methylthiophene-3-carboxylate (EMTC) is a cytotoxic agent. It inhibits the HIV virus by interfering with the synthesis of viral proteins. EMTC has been shown to be effective against cancer cells, but not against healthy cells. The cytotoxic effect of EMTC is related to its ability to inhibit DNA synthesis and RNA transcription in both normal and cancer cells, which leads to cell death.</p>

<p>3-Chloro-5-hydroxybenzoic acid methyl ester is a fine chemical that can be used as a versatile building block and reaction component in the synthesis of complex compounds. It is soluble in organic solvents such as dichloromethane, chloroform, and acetone. 3-Chloro-5-hydroxybenzoic acid methyl ester has CAS No. 98406-04-3 and a molecular weight of 149. 2.</p>

<p>Please enquire for more information about 3-Chloro-5-hydroxybenzoic acid ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2'-Chloroacetophenone is an organic compound that has been used as a hydrogen donor in the synthesis of natural products. It is produced by the reaction of acetone with chlorine gas, and it can be isolated by distillation. 2'-Chloroacetophenone reacts with hexane to form 2-chlorohexane, which can be further reacted with methanol to form methoxybenzene. The optimum concentration for this reaction is 10% (w/v) at 25°C. This chemical also has reductase activities and may enhance the activity of other reductases. 2'-Chloroacetophenone is a colorless liquid that boils at 172°C and decomposes above 300°C. It has a molecular weight of 119.16 g/mol and a density of 1.037 g/cm3 at 20°C and 0.101 g/cm3 at 25°C. It also has an intram</p>

<p>3-Chlorobenzoic acid is a compound that has been shown to have potent antibacterial activity against Pseudomonas aeruginosa and other bacteria. It has been shown to inhibit the ATP-binding cassette transporter, which is a protein that transports various molecules across cell membranes. 3-Chlorobenzoic acid also inhibits the growth of bacteria by lysing cells and interfering with DNA synthesis. This compound is an effective inhibitor of wild-type strains of E. coli, but not mutants resistant to 2,4-dichlorobenzoic acid. 3-Chlorobenzoic acid reacts with benzoate to form a crystal structure at room temperature and pressure. Further studies are needed to determine the coordination geometry and thermodynamic data for this reaction.</p>

<p>Trans-methylisoeugenol is a natural compound that has been shown to have anti-inflammatory, antioxidant, and immunomodulatory properties. It is a metabolite of isoeugenol, which is a constituent of the essential oils from plants such as angelica dahurica and eugenia caryophyllata. Trans-methylisoeugenol binds to the glucuronide conjugate receptor on the cell surface, leading to various effects including inflammatory responses. Trans-methylisoeugenol also inhibits the activity of enzymes such as benzalkonium chloride and eugenol that are responsible for inflammation. Molecular docking analysis predicts that trans-methylisoeugenol may bind to the same site on the receptor as benzalkonium chloride.</p>

<p>Boc-D-Leu-OH is a cyclic peptide that has been shown to have antibacterial activity. It is a monomer with a hydroxy group and a cavity. Boc-D-Leu-OH was found to be able to transport hydrophobic compounds across membranes, which may be due to its hydrophobic nature. Boc-D-Leu-OH also induces apoptosis in cells, which can lead to cancer. This compound has been optimized by structural modifications and residue substitutions, which have led to improved properties such as enhanced stability and increased antimicrobial activity.</p>

<p>2-Benzofurancarboxylic acid is a potent antimicrobial agent that inhibits the growth of bacteria by binding to amines, carthamus tinctorius, coumarin derivatives, and reaction mechanism. It has been shown to be effective against several types of cancer cells and autoimmune diseases. 2-Benzofurancarboxylic acid binds reversibly to the active site of an enzyme with high affinity for amines, carthamus tinctorius, coumarin derivatives, and reaction mechanism. This binding prevents the enzyme from performing its normal function.<br>2-Benzofurancarboxylic acid has also been shown to inhibit bacterial growth in a microgravity environment and was found to be more effective than its analogs in a molecular docking analysis.</p>

<p>2-(4'-Chlorobenzoyl)benzoic acid (2-CBA) is a sulfa drug that inhibits bacterial growth by blocking the synthesis of folic acid. It is also known to be luminescent and can be used in techniques such as luminescent probes. 2-CBA has antibacterial activity and can inhibit bacterial growth in a chromatographic method. 2-CBA is chemically stable and has been shown to have antibacterial properties against gram-positive bacteria, including Bacillus subtilis and Staphylococcus aureus. 2-CBA also has the ability to react with phthalazinone, an inhibitor of glutamine synthetase, which is involved in the production of ATP from ADP. This reaction results in the formation of an unstable intermediate which decomposes into CO2 and benzoic acid.</p>

<p>6-Chloroindole is a reagent that is used as a reaction component in the synthesis of organic compounds.</p>

<p>4-Chloro-8-methoxy-2-methylquinoline is a compound that has been found in nature. It is a diversity of nonreciprocal nucleic acid sequences and has been shown to be polymorphic. This nucleotide can cause stenosis in the coronary heart, which may lead to heart disease. 4-Chloro-8-methoxy-2-methylquinoline also inhibits the growth of Plasmodium falciparum and Plasmodium vivax. The drug's mechanism of action is not yet known, but it may have evolved from other compounds with a similar molecular structure.</p>

<p>(R)-1,1'-Bi-2-Naphthol is an organic compound that is made from the hydrogenation of 2-naphthol. The sodium salts of this compound are chiral and can be used to synthesize racemic mixtures with a high degree of optical purity. The x-ray crystal structures of (R)-1,1'-Bi-2-Naphthol have been studied in detail and show that this molecule exhibits intermolecular hydrogen bonding interactions. It also has a steric interaction with the amine group which prevents rotation about the C3—C4 bond. Other interesting features include intramolecular hydrogen bonding interactions between the hydroxyl group and the alkanoic acid. This molecule also has a hydrophobic region consisting of three methyl groups that are connected to fatty acids.</p>

<p>4-Cyanobenzylamine HCl is a degradable polymer that has been shown to inhibit colonic adenocarcinoma in mice. This compound was synthesized by the reaction of 4-cyanobenzylamine with 3-mercaptopropionic acid and was characterized using IR, 1H NMR, and 13C NMR spectroscopy. It also showed an inhibitory effect on the proliferation of human colon cancer cells. The polymer was found to gel when mixed with different concentrations of acrylamide and methylene bisacrylamide. Gelation occurred at a lower concentration of acrylamide than the amount used in previous studies. This may be due to its functional groups and morphology, which could have contributed to the inhibition of cell growth.</p>

<p>2-Chloroethyl methyl sulfide (2CEMS) is a reactive compound that has been shown to enhance membrane interactions and fatty acid metabolism in experimental models. 2CEMS is a substrate molecule for the reaction mechanism of the enzyme phospholipase A2, which plays an important role in the production of arachidonic acid. 2CEMS has been shown to have cytotoxic effects on 3T3-L1 preadipocytes, with cell death occurring as a result of kinetic energy emissions. The halides in 2CEMS can coordinate with hematopoietic cells, leading to the inhibition of their proliferation and differentiation. 2CEMS is also able to bind with various metals such as copper and zinc, which may be useful for pharmaceutical drug applications.</p>

<p>2-Ethoxybenzamide is a nonsteroidal anti-inflammatory drug that has been shown to inhibit the production of inflammatory prostaglandins. It is structurally similar to ethenzamide, an older drug in this class. 2-Ethoxybenzamide is used for the treatment of pain and inflammation, as well as for other conditions such as gout and rheumatoid arthritis. The molecular formula for 2-ethoxybenzamide is C6H11NO2 and its molecular weight is 169.21 grams per mole. It has a melting point of 75 degrees Celsius and a boiling point of 220 degrees Celsius at atmospheric pressure. This compound can be found in crystalline cellulose, analytical method, water vapor, experimental solubility data, wastewater treatment, ethylmalonic acid, human serum, structural analysis.</p>

<p>2-Bromo-4-iodopyridine is a coordination compound that inhibits bacterial enzyme catechol-O-methyltransferase (COMT). It is also an inhibitor of methicillin-resistant Staphylococcus aureus (MRSA) and other bacteria. 2-Bromo-4-iodopyridine binds to the active site of COMT, which is located in the bacterial cell wall, and prevents methylamine from binding to the enzyme. This prevents methylation of the catechol ring, which is required for bacterial growth. 2-Bromo-4-iodopyridine has been shown to have antimicrobial activity against Escherichia coli, Enterococcus faecalis, Bacillus subtilis, and Candida albicans.</p>

<p>1,4-Bis-(diphenylphosphino)butane is a coordination compound that contains a bicyclic heterocycle. The compounds are made up of phosphorus and nitrogen atoms which are arranged in a tetrahedral geometry. It has photochemical properties and can be used to inhibit the growth of myeloid leukemia cells. The complexes bind to amines and form stable complexes with hydroxyl groups, so they are also able to cross mitochondrial membranes. This compound has been shown to bind to copper ions in x-ray crystal structures. 1,4-Bis-(diphenylphosphino)butane binds more strongly to ethylene diamine than it does to aryl halides such as chloroethane or phenylethane. Activation energies for the binding of 1,4-bis-(diphenylphosphino)butane with ethylene diamine have been found by measuring the free energy change for its formation from</p>

1-Bromoadamantane is a quinoline derivative that binds to the inflammatory bowel disease molecule. It is used as a pharmaceutical preparation for the treatment of inflammatory bowel disease. 1-Bromoadamantane is synthesized by the palladium-catalyzed coupling reaction of 2,6-dimethoxybenzene and trifluoromethanesulfonic acid. The synthesis method involves the use of hydrochloric acid and hydroxyl group. 1-Bromoadamantane has been shown to have binding constants with ileal and colonic tissue in rats with experimental colitis.